N-Phenylsulfonylcarbamates

ABSTRACT

N-Phenylsulfonyl-N&#39;-pyrimidinyl- and -triazinylureas of the general formula ##STR1## and the salts of these compounds with amines, with alkali or alkaline-earth metal bases or with quaternary ammonium bases, have good pre- and post-emergence selective, herbicidal and growth-regulating properties. 
     The symbols in this formula are as follows: 
     A is a C 3  -C 6  -alkynyl group, 
     E is the methine group or nitrogen, 
     X is oxygen, sulfur or a sulfinyl or sulfonyl bridge, 
     Z is oxygen or sulfur, 
     m is the number one or two, 
     R 1  is hydrogen, halogen, C 1  -C 5  -alkyl or C 2  -C 5  -alkenyl or a group --Y--R 5 , 
     R 2  is hydrogen, halogen, C 1  -C 5  -alkyl, C 2  -C 5  -alkenyl or C 1  -C 4  -haloalkyl, or a group --Y--R 5 , --COOR 6 , --NO 2  or --CO--NR 7  --R 8 , 
     R 3  and R 4  independently of one another are each hydrogen, C 1  -C 4  -alkyl, C 1  -C 4  -alkoxy, C 1  -C 4  -alkylthio, C 1  -C 4  -haloalkyl, C 1  -C 4  haloalkoxy, halogen or alkoxyalkyl having at most 4 carbon atoms, 
     R 5  and R 6  are each C 1  -C 5  -alkyl, C 2  -C 5  -alkenyl or C 2  -C 6  -alkynyl, 
     R 7  and R 8  independently of one another are each hydrogen, C 1  -C 5  -alkyl, C 2  -C 5  -alkenyl or C 2  -C 6  -alkynyl, and 
     Y is oxygen, sulfur or a sulfinyl or sulfonyl bridge.

This is a division of application Ser. No. 396,959 filed on July 9, 1982 now U.S. Pat. No. 4,443,243.

The present invention relates to novel N-phenylsulfonyl-N'-pyrimidinyl- and -triazinylureas which have a herbicidal action and an action regulating plant growth, to processes for producing them, to compositions containing them as active ingredients, and also to the use thereof for combating weeds, particularly selectively in cultivated crops, or for regulating and reducing plant growth. The invention relates in addition to novel phenylsulfonamides and N-phenylsulfonylcarbamates produced as intermediates.

The N-phenylsulfonyl-N'-pyrimidinyl- and -triazinylureas according to the invention correspond to the general formula I ##STR2## wherein A is a C₃ -C₆ -alkynyl group,

E is the methine group or nitrogen,

X is oxygen, sulfur or a sulfinyl or sulfonyl bridge,

Z is oxygen or sulfur,

m is the number one or two,

R₁ is hydrogen, halogen, C₁ -C₅ -alkyl or C₂ -C₅ -alkenyl or a group --Y--R₅,

R₂ is hydrogen, halogen, C₁ -C₅ -alkyl, C₂ -C₅ -alkenyl or C₁ -C₄ -haloalkyl, or a group --Y--R₅, --COOR₆, --NO₂ or --CO--NR₇ --R₈,

R₃ and R₄ independently of one another are hydrogen, C₁ -C₄ -alkyl, C₁ -C₄ -alkoxy, C₁ -C₄ -alkylthio, C₁ -C₄ -haloalkyl, C₁ -C₄ -haloalkoxy, halogen or alkoxyalkyl having at most 4 carbon atoms,

R₅ and R₆ are each C₁ -C₅ -alkyl, C₂ -C₅ -alkenyl or C₂ -C₆ -alkynyl,

R₇ and R₈ independently of one another are each hydrogen, C₁ -C₅ -alkyl, C₂ -C₅ -alkenyl or C₂ -C₆ -alkynyl, and

Y is oxygen, sulfur or a sulfinyl or sulfonyl bridge;

and the invention relates also to the salts of these compounds.

Urea compounds, triazine compounds and pyrimidine compounds having herbicidal activity are known in general. There have recently been described arylsulfamoyl-heterocyclyl-aminocarbamoyl compounds having a herbicidal action and an action regulating plant growth, for example in the European Patent Publications Nos. 1514 and 1515, in the U.S. Patent Specification No. 4,127,405, the German Offenlegungsschrift No. 2,715,786 and the French Patent Specification No. 1,468,747.

Alkyl in the definitions is straight-chain or branched-chain alkyl, for example methyl, ethyl, n-propyl, i-propyl, the four isomeric butyl groups, n-amyl, i-amyl, 2-amyl, 3-amyl, n-hexyl or i-hexyl.

By alkoxy is meant: methoxy, ethoxy, n-propyloxy, i-propyloxy and the four isomeric butyloxy groups, in particular however methoxy, ethoxy or i-propoxy.

Examples of alkylthio are: methylthio, ethylthio, n-propylthio, i-propylthio and n-butylthio, but especially methylthio and ethylthio.

Examples of alkenyl groups are: vinyl, allyl, isopropenyl, 1-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-isobutenyl, 2-isobutenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl and 4-pentenyl, particularly however, vinyl, allyl and 4-pentenyl.

Examples of alkylsulfinyl are: methylsulfinyl, ethylsulfinyl, n-propylsulfinyl and n-butylsulfinyl, especially methylsulfinyl and ethylsulfinyl.

Examples of alkylsulfonyl are: methylsulfonyl, ethylsulfonyl, n-propylsulfonyl and n-butylsulfonyl, particularly however methylsulfonyl and ethylsulfonyl.

Halogen in the definitions, as well as in haloalkyl, --alkoxy, --alkylsulfonyl, --alkylsulfonyl and --alkylthio, is fluorine, chlorine and bromine, preferably fluorine and chlorine.

Alkynyl groups in the definitions of the above symbols are as a rule: propargyl, 2-butynyl and 3-butynyl, as well as isomeric pentynyl or hexynyl groups; the alkynyl group is preferably however propargyl or 2- or 3-butynyl.

The invention embraces also the salts which the compounds of the formula I can form with amines, alkali metal bases and alkaline-earth metal bases or quaternary ammonium bases. To be emphasised among the alkali metal and alkaline-earth metal hydroxides as salt formers are the hydroxides of lithium, sodium, potassium, magnesium or calcium, especially however of sodium or potassium. Examples of amines suitable for forming salts are: primary, secondary and tertiary aliphatic and aromatic amines, such as methylamine, ethylamine, propylamine, i-propylamine, the four isomeric butylamines, dimethylamine, diethylamine, diethanolamine, dipropylamine, diisopropylamine, di-n-butylamine, pyrrolidine, piperidine, morpholine, trimethylamine, triethylamine, tripropylamine, quinuclidine, pyridine, quinoline and i-quinoline, in particular however ethyl-, propyl-, diethyl- or triethylamine, but especially isopropylamine and diethanolamine. Examples of quaternary ammonium bases are in general the cations of haloammonium salts, for example the tetramethylammonium cation, the trimethylbenzylammonium cation, the triethylbenzylammonium cation, the tetraethylammonium cation or the trimethylethylammonium cation, but also the ammonium cation.

Preferred compounds of the formula I are those in which

(a) Z is oxygen, and

(b) R₃ and R₄ together contain no more than 4 carbon atoms.

The group (a) can be divided into two further subgroups consisting of compounds in which

(aa) m is the number one, and

(ab) m is the number two.

Preferred compounds from the group (aa) are those in which the group --X--A is in the 2- or 3-position with respect to the sulfonyl group. Compounds particularly preferred in this group are those wherein the group --X--A is in the 2-position.

A preferred group from the group (ab) is formed by the compounds in which the two --X--A groups are in the 2- and 5-positions with respect to the sulfonyl group.

A further preference with regard to compounds of the aforementioned subgroups of the groups (aa) and (ab) is that R₃ and R₄ together contain at most 4 carbon atoms. There are thus formed the especially preferred groups of compounds of the formula I wherein

(aab) only one --X--A group is present in the 2-position with respect to the sulfonyl group, Z is oxygen, and R₃ and R₄ together contain no more than 4 carbon atoms atoms, and

(abb) two --X--A groups are present in the 2- and 5-position with respect to the sulfonyl group, Z is oxygen, and R₃ and R₄ together contain no more than 4 carbon atoms.

Preferred compounds from the group (aab) are those in which R₁ is hydrogen, and R₂ is in the 5- or 6-position with respect to the sulfonyl grouop. And of these compounds moreover, those are preferred in which R₂ is hydrogen, halogen, C₁ -C₄ -alkoxy, nitro or COOR₆.

A further preference within the last-mentioned group is for the compounds in which R₂ is hydrogen, fluorine, nitro or C₁ -C₄ -alkoxy, and R₃ and R₄ are each hydrogen, C₁ -C₄ -alkyl, C₁ -C₄ -alkoxy, C₁ -C₄ -alkylthio, C₁ -C₃ -haloalkoxy, halogen or alkoxyalkyl, where R₃ and R₄ together contain no more than 4 carbon atoms.

Compounds among these which are in their turn preferred are those in which R₂ is hydrogen, and R₃ and R₄ are each C₁ -C₄ -alkyl, C₁ -C₄ -alkoxy, methylthio, 2,2,2-trifluoroethoxy, difluoromethoxy, 1,1,2,2-tetrafluoroethoxy, halogen or alkoxyalkyl. A further preference within the lastmentioned group is for the compounds in which X is oxygen or sulfur. More especially preferred of these, however, are the compounds in which X is oxygen. Preferred compounds within this group are those in which A is propargyl.

Of the compounds of the formula I wherein Z is sulfur, those are preferred in which X is oxygen or sulfur, R₃ and R₄ independently of one another are each C₁ -C₃ -alkyl, C₁ -C₃ -alkoxy, C₁ -C₃ -alkylthio, difluoromethoxy or 2,2,2-trifluoroethoxy, with together at most 4 carbon atoms, and A is --CH₂ --C.tbd.CH, --CH₂ --C.tbd.C--CH₃ or --CH₂ CH₂ C.tbd.CH, and the --X--A group occupies the 2-position, and m is the number 1.

The following are given as preferred individual compounds:

N-(2-propargyloxyphenyl-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-urea,

N-(2-propargyloxyphenyl-sulfonyl)-N'-(4-ethyl-6-methoxy-1,3,5-triazin-2-yl)-urea,

N-(2-propargyloxyphenyl-sulfonyl)-N'-(4,6-dimethoxy-1,3,5-triazin-2-yl)-urea, and

N-(2-propargyloxyphenyl-sulfonyl)-N'-(4-ethoxy-6-methyl-1,3,5-triazin-2-yl)-urea.

The compounds of the formula I are produced in an inert organic solvent.

One process for producing the compounds of the formula I comprises reacting a phenylsulfonamide of the formula II ##STR3## wherein A, R₁, R₂, X and m have the meanings defined under the formula I, in the presence of a base, with an N-pyrimidinyl- or -triazinylcarbamate of the formula III ##STR4## wherein E, R₃, R₄ and Z have the meanings defined under the formula I.

Compounds of the formula I are obtained, using a second process, by reacting a phenylsulfonylisocyanate or -isothiocyanate of the formula IV ##STR5## wherein A, R₁, R₂, m, X and Z are as defined under the formula I, optionally in the presence of a base, with an amine of the formula V ##STR6## wherein E, R₃ and R₄ have the meanings defined under the formula I.

Compounds of the formula I are produced in a further process by reacting a sulfonamide of the formula II given above, optionally in the presence of a base, with an isocyanate or isothiocyanate of the formula VI ##STR7## wherein E, R₃, R₄ and Z are as defined under the formula I.

Finally, the compounds of the formula I can be obtained also by reacting an N-phenylsulfonylcarbamate of the formula VII ##STR8## wherein A, R₁, R₂, m, X and Z have the meanings defined under the formula I, with an amine of the above formula V.

The resulting ureas of the formula I can if desired be converted, by means of amines, alkali metal or alkaline-earth metal hydroxides or quaternary ammonium bases, into addition salts. This is effected for example by reaction with the equimolar amount of a base, and removal of the solvent by evaporation.

The starting materials of the formulae II, IV and VII are novel and can be produced by the following methods.

The novel sulfonamides of the formula II which are used as intermediates are obtained from the corresponding anilines by diazotisation and exchange of the diazo group for sulfur dioxide in the presence of a catalyst, such as copper-I chloride, in hydrochloric acid or acetic acid, and reaction of the formed phenylsulfonyl chloride with ammonia.

The compounds of the formula I can be obtained also by oxygen- or sulfur-alkynylation of hydroxy- or thiophenylsulfonamides with the corresponding halides or sulfuric acid esters, or by reaction of ortho-halophenylsulfonamides with metal alcoholates or mercaptides, and optionally by oxidation thereof with for example periodates or peroxy acids to the corresponding sulfoxides and sulfones.

Ortho-substituted hydroxyphenyl- or substituted ortho-hydroxyphenylsulfonamides of the formula VIII ##STR9## wherein R₁ and R₂ have the meanings defined under the formula I, and X' is oxygen or sulfur, are known, as starting products of certain sulfonamide representatives of the formula II, from the Swiss Patent Application No. 3991/81-4. They can be obtained by ether cleavage of the corresponding C₁ -C₄ -alkoxyphenylsulfonamides for example with boron trihalides (reactions of this type are described in the U.S. Pat. No. 3,904,680 and in J. Am. Chem. Soc. 64, 1128 (1942)), or by hydrogenolysis of the corresponding benzyloxyphenylsulfonamides, as described in J. Chem. Soc. 1958, 2903.

The alkoxyphenylsulfonamides for their part can be obtained from the corresponding alkoxyanilides, as already mentioned, or by chlorosulfonylation of alkoxybenzenes by reaction of the resulting phenylsulfonyl chlorides with ammonia. Such reactions have become known from J. Am. Chem. Soc. 62, 603 (1940).

The compounds of the formula II and VII used as intermediates are novel and were developed specifically for the synthesis of compounds of the formula I. These intermediates form further subject matter of the present invention.

The phenylsulfonylisocyanates of the formula IV can be obtained by reaction of the sulfonamides of the formula II with phosgene in the presence of butylisocyanate, in a chlorinated hydrocarbon as solvent, at reflux temperature. Similar production methods are described in "Neuere Methoden der pr/a/ parativen organischen Chemie", Vol. VI, 211-229, Verlag Chemie, Weinheim, 1970.

The isothiocyanates of the formula IV are obtained by treatment of the sulfonamides of the formula II with carbon disulfide and potassium hydroxide, and subsequent reaction of the dipotassium salt with phosgene. Processes of this kind are described in Arch. Pharm. 299, 174 (1966).

The N-phenylsulfonylcarbamates of the formula VII are obtained by reaction of the sulfonamides of the formula II with diphenylcarbonate in the presence of a base. Similar processes are mentioned in the Japanese Patent Specification No. 61 169.

The starting materials of the formulae III, V and VI are in part known. New compounds of the formulae III and VI can be obtained, by known methods, from corresponding compounds of the formula V.

New fluoroalkoxy-aminopyrimidines and -triazines of the formula V and the production thereof, and also the production therefrom of corresponding compounds of the formulae III and VI, are described in the Swiss Patent Application No. 3527 /82-8.

Isocyanates of the formula VI can be produced by reaction of amines of the formula V with oxalyl chloride in chlorinated hydrocarbons as solvents. Amines of the formula V are known and some are obtainable commercially, or they can be produced by known methods (cp. "The Chemistry of Heterocyclic Compounds", Vol. XIV, Interscience Publishers, New York, London.

These reactions to give compounds of the formula I are advantageously performed in aprotic, inert, organic solvents, such as methylene chloride, tetrahydrofuran, acetonitrile, dioxane and toluene.

The reaction temperatures are preferably between -20° and +120° C. The reactions proceed in general slightly exothermically, and can be carried out at room temperature. For the purpose of shortening the reaction time or for initiating the reaction, it is advantageous to apply heat for a short time up to the boiling point of the reaction mixture. The reaction times can be shortened also by the addition of some drops of a base or of isocyanate as a reaction catalyst.

The final products can be isolated by concentration by evaporation and/or by removal of the solvent by evaporation, and purified by recrystallization or trituration of the solid residue in solvents in which they do not readily dissolve, such as ether, aromatic hydrocarbons or chlorinated hydrocarbons.

The active substances of the formula I are stable compounds, and the handling of them necessitates no special precautions being taken.

In smaller applied amounts, the compounds of the formula I are characterised by good selective growth-inhibiting and selective herbicidal properties, which render them excellently suitable for use in crops of useful plants, especially in crops of cereals, cotton, soya-bean, maize and rice. The preferred crops are cereals, such as wheat, barley and rye. Also destroyed in some cases are weeds which hitherto could be dealt with only by the use of total herbicides.

The mode of action of these active substances is unusual. Many are capable of being translocated, that is to say, they are taken up by the plant and transported to other locations, where they produce the desired effect. It is thus possible for example by surface treatment of perennial weeds to destroy them at their roots. The novel compounds of the formula I are effective in applied amounts which are very small compared with the amounts required to obtain the same effect using other herbicides and plant-growth regulators.

The compounds of the formula I also have excellent properties for regulating, especially reducing, plant growth. Both monocotyledons and dicotyledons are impaired in their growth. A reduction of the vegetative growth enables in the case of many cultivated plants the crop density to be raised, so that higher yields for the same area of land can be achieved.

An additional factor contributing to the increase in yield with the use of growth inhibitors is that the formation of blossom and fruit benefits to a greater extent from the nutritive substances, because the vegetative growth is restricted.

Thus, for example, the leguminosae frequently planted as cover crops in agriculture in tropical regions are selectively inhibited in their growth by the compounds of the formula I, the result being that soil erosion between the cultivated plants is prevented, without the cover crops being able to compete with the main cultivated crop.

Furthermore, the compounds of the formula I are suitable for preventing the sprouting of stored potatoes. Shoots frequently form on potatoes being stored during the winter, and the shoots cause shrinkage, loss in weight and rotting.

With larger applied amounts of active substance, all the tested plants were impaired in their development to the extent that they died.

The invention relates also to herbicidal and plant-growth-regulating compositions containing a novel active ingredient of the formula I, and also to processes for the pre- and post-emergence combating of weeds, and for the reduction of growth of monocotyledonous and dicotyledonous plants, particularly that of grasses, tropical cover crops and side shoots of tobacco plants.

The compounds of the formula I are used either in an unmodified form or preferably in compositions, together with auxiliaries customarily employed in formulation practice, and are thus processed, in a known manner, for example into the form of emulsion concentrates, directly sprayable or dilutable solutions, diluted emulsions, wettable powders, soluble powders, dusts or granulates, and also encapsulations in for example polymeric substances. The application processes, such as spraying, atomising, dusting, scattering or pouring, and likewise the type of composition, are selected to suit the objects to be achieved and the given conditions.

The formulations, that is to say, the compositions or preparations containing the active ingredient of the formula I and optionally a solid or liquid additive, are produced in a known manner, for example by the intimate mixing and/or grinding of the active ingredients with extenders, such as with solvents, solid carriers and optionally surface-active compounds (tensides).

Suitable solvents are: aromatic hydrocarbons, preferably the fractions C₈ to C₁₂, such as xylene mixtures or substituted naphthalenes, phthalic esters, such as dibutyl- or dioctylphthalate, aliphatic hydrocarbons, such as cyclohexane or paraffins, alcohols and glycols, as well as ethers and esters thereof, such as ethanol, ethylene glycol, ethylene glycol monomethyl or -ethyl ethers, ketones, such as cyclohexanone, strongly polar solvents, such as N-methyl-2-pyrrolidone, dimethylsulfoxide or dimethylformamide, as well as optionally epoxidised vegetable oils, such as epoxidised coconut oil or soybean oil; or water.

The solid carriers used, for example for dusts and dispersible powders, are as a rule natural mineral fillers, such as calcite, talcum, kaolin, montmorillonite or attapulgite. In order to improve the physical properties, it is also possible to add highly dispersed silicic acid or highly dispersed absorbent polymers. Suitable granulated adsorptive carriers are porous types, for example pumice, ground brick, sepiolite or bentonite; and suitable nonsorbent carriers are materials such as calcite or sand. There can also be used a great number of pre-granulated materials of inorganic or organic nature, such as in particular dolomite or ground plant residues.

Suitable surface-active compounds are, depending on the nature of the active substance of the formula I to be formulated, nonionic, cationic and/or anionic tensides having good emulsifying, dispersing and wetting properties. By `tensides` are also meant mixtures of tensides.

Suitable anionic tensides are both so-called water-soluble soaps as well as water-soluble, synthetic, surface-active compounds.

Soaps which are applicable are the alkali metal, alkaline-earth metal or optionally substituted ammonium salts of higher fatty acids (C₁₀ -C₂₂), for example the Na or K salts of oleic or stearic acid, or of natural fatty acid mixtures, which can be obtained for example from coconut oil or tallow oil. Also to be mentioned are the fatty acid-methyl-taurine salts.

So-called synthetic tensides are however more frequently used, particularly fatty sulfonates, fatty sulfates, sulfonated benzimidazole derivatives or alkylarylsulfonates. The fatty sulfonates or sulfates are as a rule in the form of alkali metal, alkaline-earth metal or optionally substituted ammonium salts, and contain an alkyl group having 8 to 22C atoms, `alkyl` including also the alkyl moiety of acyl groups, for example the Na or Ca salt of ligninsulfonic acid, of dodecylsulfuric acid ester or of a fatty alcohol sulfate mixture produced from natural fatty acids. Included among these are also the salts of sulfuric acid esters and sulfonic acids of fatty alcohol ethylene oxide adducts. The sulfonated benzimidazole derivatives preferably contain 2 sulfonic acid groups and a fatty acid group having 8-22C atoms. Alkylarylsulfonates are for example the Na, Ca or triethanolamine salts of dodecylbenzenesulfonic acid, of dibutylnaphthalenesulfonic acid or of a naphthalenesulfonic acid-formaldehyde condensation product. Also suitable are corresponding phosphates, for example salts of the phosphoric ester of a p-nonylphenol-(4-14)-ethylene oxide adduct.

Suitable nonionic tensides are in particular polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, saturated or unsaturated fatty acids and alkylphenols, which can contain 3 to 30 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon radical and 6 to 18 carbon atoms in the alkyl moiety of the alkylphenols.

Further suitable nonionic tensides are the water-soluble polyethylene oxide adducts, which contain 20 to 250 ethylene glycol ether groups and 10 to 100 propylene glycol ether groups, with polypropylene glycol, ethylene-diaminopolypropylene glycol and alkylpolypropylene glycol having 1 to 10 carbon atoms in the alkyl chain. The compounds mentioned usually contain 1 to 5 ethylene glycol units per propylene glycol unit. Examples of nonionic tensides which may be mentioned are: nonylphenolpolyethoxyethanols, castor oil polyglycol ethers, polypropylene/polyethyleneoxy adducts, tributylphenoxypolyethoxyethanol, polyethylene glycol and octylphenoxypolyethoxyethanol. Suitable also are fatty acids esters of polyoxyethylenesorbitan, such as polyoxyethylenesorbitan-trioleate.

In the case of the cationic tensides, they are in particular quaternary ammonium salts which contain as N-substituents at least one alkyl group having 8 to 22C atoms and, as further substituents, lower, optionally halogenated alkyl, benzyl or lower hydroxyalkyl groups. The salts are preferably in the form of halides, methyl sulfates or ethyl sulfates, for example stearyltrimethylammonium chloride or benzyldi(2-chloroethyl)ethylammonium bromide.

The tensides customarily used in formulation practice are described, inter alia, in the following publications:

"Mc Cutcheon's Detergents and Emulsifiers Annual" MC Publishing Corp., Ridgewood, N.J., 1979; and Sisley and Wood, "Encyclopedia of Surface Active Agents", Chemical Publishing Co., Inc. New York, 1964.

The agrochemical preparations contain as a rule 0.1 to 95%, especially 0.1 to 80%, of active ingredient of the formula I, 1 to 99.9% of a solid or liquid additive, and 0 to 25%, particularly 0.1 to 25%, of a tenside.

Preferred formulations are made up in particular as follows (%=percent by weight):

Emulsifiable concentrates

active ingredient: 1 to 20%, preferably 5 to 10%

surface active agent: 5 to 30%, preferably 10 to 20%

liquid carrier: 50 to 94%, preferably 70 to 85%.

Dusts

active ingredient: 0.1 to 10%, preferably 0.1 to 1%

solid carrier: 99.9 to 90% preferably 99.9 to 99%.

Suspension concentrates

active ingredient: 5 to 75%, preferably 10 to 50%

water: 94 to 25%, preferably 90 to 30%

surface-active agent: 1 to 40%, preferably 2 to 30%.

Wettable powders

active ingredient: 0.5 to 90%, preferably 1 to 80%

surface-active agent: 0.5 to 20%, preferably 1 to 15%

solid carrier: 5 to 95%, preferably 15 to 90%.

Granulates

active ingredient: 0.5 to 30%, preferably 3 to 15%

solid carrier: 99.5 to 70%, preferably 97 to 85%.

Whereas commercial products are preferably in the form of concentrated compositions, the compositions employed by the end-user are as a rule diluted. The preparations can for application be diluted down to 0.001% of active ingredient. The applied amounts are usually 0.01 to 10 kg, preferably 0.025 to 5, kg of active substance per hectare.

The compositions can also contain additives such as stabilisers, antifoaming agents, viscosity regulators, binders and adhesives, as well as fertilisers or other active substances for obtaining special effects.

In the following Examples, the temperatures are given in degrees Centigrade (°C.), and pressures in millibars (mb).

PRODUCTION EXAMPLES EXAMPLE 1

(a) 2-Propargyloxyphenylsulfonamide:

A mixture of 35 g of 2-hydroxyphenylsulfonamide, 55.2 g of potassium carbonate, 15.5 ml of propargyl bromide and 1000 ml of ethyl methyl ketone is refluxed for 1.5 hours; it is then cooled, filtered, and concentrated by evaporation. The yield after recrystallisation of the residue from ethyl acetate is 30 g of 2-propargyloxyphenylsulfonamide, m.p. 143°-145° C.

(b) N-(2-Propargyloxyphenylsulfonyl)-phenyl carbamate:

A solution of 15.1 g of 2-propargyloxyphenylsulfonamide in 100 ml of dimethylformamide is added dropwise within 10 minutes, at a maximum temperature of 10° C. in a nitrogen atmosphere, to the suspension of 3.09 g of 55% sodium hydride in 30 ml of absolute dimethylformamide. The reaction mixture is stirred for 15 minutes at room temperature; there is subsequently added dropwise, in the course of 20 minutes, a solution of 15.94 g of diphenyl carbonate in 100 ml of dimethylformamide, and the mixture is stirred for a further 45 minutes. The reaction mixture is afterwards taken up in a mixture of 600 g of ice, 90.5 ml of 2N hydrochloric acid and 600 ml of ethyl acetate. The organic phase is washed twice with ice water, dried over sodium sulfate and concentrated by evaporation. Ether/petroleum ether (1:1) is added to the oily residue to thus obtain 21.4 g of crystalline N-(2-propargyloxyphenylsulfonyl)-phenyl carbamate, m.p. 155°-157° C.

(c) N-(2-Propargyloxyphenylsulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-urea:

A mixture of 3.33 g of N-(2-propargyloxyphenylsulfonyl)-phenyl carbamate and 1.4 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine in 30 ml of absolute dioxane is refluxed for 45 minutes; the mixture is then cooled to room temperature, filtered, and concentrated by evaporation. The yield after trituration of the residue with 40 ml of ether is 2.38 g of crystalline N-(2-propargyloxyphenylsulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-urea, m.p. 157°-158° C.

EXAMPLE 2

(a) 5-Methyl-2-propargyloxyphenylsulfonamide:

A mixture of 24.3 g of 2-hydroxy-5-methylphenylsulfonamide, 36.0 g of potassium carbonate, 16.7 g of propargyl bromide and 500 ml of acetonitrile is stirred at 50° C. for 4.5 hours. The reaction mixture is then filtered, and concentrated by evaporation. The yield after recrystallisation from ethyl acetate is 23.9 g of 5-methyl-2-propargyloxyphenylsulfonamide, m.p. 169°-170° C.

(b) 5-Methyl-2-propargyloxyphenylsulfonylisocyanate:

A mixture of 22.4 g of 5-methyl-2-propargyloxyphenylsulfonamide, 9.9 g of n-butylisocyanate, 0.3 g of 1,4-diazabicyclo(2,2,2)octane and 350 ml of absolute xylene is refluxed for 30 minutes; and about 20 g of phosgene are subsequently introduced at 115°-120° C. during 2 hours. After the excess of phosgene has been removed from the reaction mixture by feeding in nitrogen, the mixture is cooled to room temperature, filtered, and concentrated in vacuo. There is thus obtained as crude product 28.1 g of 5-methyl-2-propargyloxyphenylsulfonylisocyanate in the form of brown oil. This crude product is used, without further purification, in the subsequent stage.

(c) N-(5-Methyl-2-propargyloxyphenylsulfonyl)-N'-(4-chloro-6-methoxypyrimidin-2-yl)-urea:

A solution of 9.4 g of crude 5-methyl-2-propargyloxyphenylsulfonylisocyanate in 50 ml of absolute tetrahydrofuran is added dropwise at room temperature, within 10 minutes, to a solution of 3.7 g of 2-amino-4-chloro-6-methoxy-pyrimidine and 0.1 g of 1,4-diazadicyclo[2,2,2]octane in 60 ml of absolute tetrahydrofuran, in the course of which the temperature rises slightly. The reaction solution is carried for 18 hours at room temperature; it is then filtered, and concentrated by evaporation. The residue is crystallised from ethyl acetate to thus obtain 5.8 g of N-(5-methyl-2-propargyloxyphenylsulfonyl)-N'-(4-chloro-6-methoxy-pyrimidin-2-yl)-urea, m.p. 202°-204° C.

The intermediate and final products listed in the following Tables are obtained in an analogous manner.

                                      TABLE 1     __________________________________________________________________________      ##STR10##                                  Position                                       Physical     R.sub.1 R.sub.2                   X  A           of XA                                       data     __________________________________________________________________________     H       H     O  CH.sub.2CCH 2    m.p. 143-145°     H       H     S  CH.sub.2CCH 2     H       H     O  CH.sub.2CH.sub.2CCH                                  2     H       H     O  CH.sub.2CCCH.sub.3                                  2     6-Cl    H     O  CH.sub.2CCH 2     6-Cl    H     O  CH.sub.2CCCH.sub.3                                  2     6-Cl    H     O  CH.sub.2CH.sub.2CCH                                  2     6-OCH.sub.3             H     O  CH.sub.2CCH 2     6-OCH.sub.3             H     O  CH.sub.2CCCH.sub.3                                  2     6-CH.sub.3             H     O  CH.sub.2CCH 2     6-CH.sub.3             H     O  CH.sub.2CH.sub.2CCH                                  2     6-NO.sub.2             H     O  CH.sub.2CCH 2     6-NO.sub.2             H     O  CH.sub.2CCCH.sub.3                                  2     6-COOCH.sub.3             H     O  CH.sub.2CCH 2     5-Cl    H     O  CH.sub.2CCH 2    m.p. 145°     5-Cl    H     O  CH.sub.2CH.sub.2CCH                                  2     5-Cl    H     O  CH.sub.2CCCH.sub.3                                  2     5-Br    H     O  CH.sub.2CCH 2     5-Br    H     O  CH.sub.2CCCH.sub.3                                  2     5-Br    H     O  CH.sub.2CH.sub.2CCH                                  2     5-F     H     O  CH.sub.2CCH 2    m.p. 156-157°     5-F     H     O  CH.sub.2CH.sub.2CCH                                  2     5-F     H     O  CH.sub.2CCCH.sub.3                                  2     5-CH(CH.sub.3).sub.2             H     O  CH.sub.2CCH 2     5-CH(CH.sub.3).sub.2             H     O  CH.sub.2CH.sub.2CCH                                  2     5-CH(CH.sub.3).sub.2             H     O  CH.sub.2C CCH.sub.3                                  2     5-CH.sub.3             H     O  CH.sub.2CCH 2    m.p. 169-171°     5-CH.sub.3             H     O  CH.sub.2CCCH.sub.3                                  2     5-CH.sub.3             H     O  CH.sub.2CH.sub.2CCH                                  2     5-NO.sub.2             H     O  CH.sub.2CCH 2     5-NO.sub.2             H     O  CH.sub.2CH.sub.2CCH                                  2     5-NO.sub.2             H     O  CH.sub.2CCCH.sub.3                                  2     5-OCH.sub.3             H     O  CH.sub.2CCCH.sub.3                                  2     5-OCH.sub.3             H     O  CH.sub.2CCH 2     5-OCH.sub.3             H     O  CH.sub.2CH.sub.2CCH                                  2     5-CON(CH.sub.3).sub.2             H     O   CH.sub.2CCH                                  2     5-CON(CH.sub.3).sub.2             H     O  CH.sub.2CCCH.sub.3                                  2     5-COOCH.sub.3             H     O  CH.sub.2CCH 2     5-COOCH.sub.3             H     O  CH.sub.2CCCH.sub.3                                  2     5-COOCH.sub.3             H     O  CH.sub.2CH.sub.2CCH                                  2     5-NO.sub.2             3-CF.sub.3                   O  CH.sub.2CCH 2     5-NO.sub.2             3-Cl  O  CH.sub.2CCH 2     5-NO.sub.2             3-Cl  O  CH.sub.2CCCH.sub.3                                  2     5-CF.sub.3             3-NO.sub.2                   O  CH.sub.2CCH 2     5-CH.sub.3             3-CH.sub.3                   O  CH.sub.2CCH 2     5-CH.sub.3             3-CH.sub.3                   O  CH.sub.2CH.sub.2CCH                                  2     5-Cl    3-NO.sub.2                   O  CH.sub.2CCH 2     5-Cl    3-Cl  O  CH.sub.2CCH 2     5-Cl    3-Cl  O  CH.sub.2CCCH.sub.3                                  2     5-Cl    3-Cl  O  CH.sub.2CH.sub.2CCH                                  2     5-Br    3-OCH.sub.3                   O  CH.sub.2CCH 2     5-Br    2-OCH.sub.3                   O  CH.sub.2CCH 3     3-OCH.sub.3             5-COOCH.sub.3                   O  CH.sub.2CCH 2     2-OCH.sub.3             5-COOCH.sub.3                   O  CH.sub.2CCH 3     5-CH.sub.3             3-Br  O  CH.sub.2CCH 2     5-Br    3-NO.sub.2                   O  CH.sub. 2CCH                                  2     5-Cl    3-Br  O  CH.sub.2CCH 2     5-Cl    3-Br  O  CH.sub.2CCCH.sub.3                                  2     5-Cl    3-Br  O  CH.sub.2CH.sub.2CCH                                  2     5-CH(CH.sub.3).sub.2             3-CH.sub.3                   O  CH.sub.2CH.sub.2CCH                                  2     5-CH(CH.sub.3).sub.2             3-CH.sub.3                   O  CH.sub.2CCCH.sub.3                                  2     5-CH(CH.sub.3).sub.2             3-CH.sub.3                   O  CH.sub.2CCH 2     3-NO.sub.2             H     O  CH.sub.2CCH 2     3-CH.sub.3             H     O  CH.sub.2CCH 2     3-NO.sub.2             H     O  CH.sub.2CCH 2     3-Cl    H     O  CH.sub.2CCH 2     3-Cl    H     O  CH.sub.2CCCH.sub.3                                  2     3-Cl    H     O  CH.sub.2CH.sub.2CCH                                  2     3-OCH.sub.3             H     O  CH.sub.2CCH 2     3-OCH.sub.3             H     O  CH.sub.2CCCH.sub.3                                  2     2-OCH.sub.3             H     O  CH.sub.2CCH 2     H       H     SO CH.sub.2CCH 2     H       H     SO.sub.2                      CH.sub.2CCH 2     H       H     SO CH.sub.2CCCH.sub.3                                  2     H       H     SO.sub.2                      CH.sub.2CCCH.sub.2                                  2     2-Cl    H     O  CH.sub.2C CH                                  5    m.p. 149°     6-Cl    4-Br  o  CH.sub.2CCH 3    m.p. 174°     __________________________________________________________________________

                                      TABLE 2     __________________________________________________________________________      ##STR11##     No.          A         R.sub.3 R.sub.4       X  E  Physical data     __________________________________________________________________________     1  CH.sub.2CCH CH.sub.3                            C.sub.2 H.sub.5                                          S  N     2  CH.sub.2CCH OCH.sub.3                            C.sub.2 H.sub.5                                          S  N     3  CH.sub.2CCH CH.sub.3                            OCH.sub.3     S  CH     4  CH.sub.2CCH OCH.sub.3                            OCH.sub.3     S  CH     5  CH.sub.2C CH                    CH.sub.3                            OCH.sub.3     SO N     6  CH.sub.2CCH OCH.sub.3                            OCH.sub.3     SO N     7  CH.sub.2CCH OCH.sub.3                            C.sub.2 H.sub.5                                          SO N     8  CH.sub.2CCH CH(CH.sub.3).sub.2                            OCH.sub.3     O  CH m.p. 129-130°     9  CH.sub.2CCH OCH.sub.3                            SC.sub.2 H.sub.5                                          O  CH     10 CH.sub.2CCH OCH.sub.3                            SC.sub.2 H.sub.5                                          O  N     11 CH.sub.2CCH OCH.sub.3                            SCH(CH.sub.3).sub.2                                          O  N     12 CH.sub.2CCH CCl     CH.sub.3      O  N  m.p. 179-180°     13 CH.sub.2CCH CH.sub.3                            Br            O  N     14 CH.sub.2CCH CHF.sub.2                            OCH.sub.3     O  N  m.p. 166-167°     15 CH.sub.2CCH CHF.sub.2                            CH.sub.3      O  N     16 CH.sub.2CCH OCH.sub.2 CF.sub.3                            Cl            O  N     17 CH.sub.2CCH OCH.sub.2 CF.sub.3                            OCH.sub.3     O  N  m.p. 113-115°     18 CH.sub.2CCH CH.sub.2 CF.sub.3                            CH.sub.3      O  N     19 CH.sub.2CCH OC.sub.2 H.sub.5                            OC.sub.2 H.sub.5                                          O  N  m.p. 138-139°     20 CH.sub.2CCH OC.sub.2 H.sub.5                            OC.sub.2 H.sub.5                                          O  CH     21 CH.sub.2CCH C.sub.2 H.sub.5                            OCH.sub.3     O  N  m.p. 134-135°     22 CH.sub.2CCH C.sub.2 H.sub.5                            OC.sub.2 H.sub.5                                          O  N     23 CH.sub.2CCH CH.sub.3                            OC.sub.2 H.sub.5                                          O  N  m.p. 129-130°     24 CH.sub.2CCH CH.sub.3                            CH.sub.3      O  CH     25 CH.sub.2CCH CH.sub.3                            OCH.sub.3     O  CH m.p. 156-159°     26 CH.sub.2CCH CH.sub.3                            OCH.sub.2CF.sub.3                                          O  N     27 CH.sub.2CCH CH.sub.3                            H             O  N  m.p. 186-187°     28 CH.sub.2CCH C.sub.2 H.sub.5                            Cl            O  CH     29 CH.sub.2CCH CH.sub.3                            Cl            O  CH m.p. 225-227°     30 CH.sub.2CCH CH.sub. 3                            SCH.sub.3     O  CH     31 CH.sub.2CCH CH.sub.3                            F             O  CH     32 CH.sub.2CCH CH.sub.3                            Br            O  CH     33 CH.sub.2CCH C.sub.2 H.sub.5                            OC.sub.2 H.sub.5                                          O  CH     34 CH.sub.2CCH C.sub.2 H.sub.5                            SCH.sub.3     O  CH     35 CH.sub.2CCH CF.sub.3                            CH.sub.3      O  CH     36 CH.sub.2CCH CH.sub.2 Cl                            CH.sub.3      O  CH     37 CH.sub.2CCH CH.sub.2 Cl                            OCH.sub.3     O  CH     38 CH.sub.2CCH OCH.sub.3                            Cl            O  CH m.p. 209-210°     39 CH.sub.2CCH Cl      Cl            O  CH     40 CH.sub.2CCH OCH.sub.3                            SCH.sub.3     O  CH     41 CH.sub.2CCH OCH.sub.3                            OCH(CH.sub.3).sub.2                                          O  CH     42 CH.sub.2CCH CH.sub.2 F                            OCH.sub.3     O  CH     43 CH.sub.2CCH CHF.sub.2                            CH.sub.3      O  CH m.p. 189-192°     44 CH.sub.2CCH CF.sub.3                            OCH.sub.3     O  CH     45 CH.sub.2CCH C.sub.2 H.sub.5                            OCH(CH.sub.3).sub.2                                          O  N     46 CH.sub.2CCH C.sub.2 H.sub.5                            Cl            O  N     47 CH.sub.2CCH C.sub.2 H.sub.5                            SCH.sub.3     O  N     48 CH.sub.2CCH C.sub.2 H.sub.5                            CH.sub.3      O  N  m.p. 132-134°     49 CH.sub.2CCH C.sub.2 H.sub.5                            C.sub.2 H.sub.5                                          O  N     50 CH.sub.2CCH OCH.sub.3                            OCH(CH.sub.3).sub.2                                          O  N  m.p.  93-95°     51 CH.sub.2CCH OCH.sub.3                            OCH(CH.sub.3)CH.sub.2CH.sub.3                                          O  N     52 CH.sub.2CCH CH.sub.3                            CH(CH.sub.3).sub.2                                          O  N     53 CH.sub.2CCH CH(CH.sub.3).sub.2                            Cl            O  N  m.p. 120-121°     54 CH.sub.2CCH CH(CH.sub.3).sub.2                            OCH.sub.3     O  N     55 CH.sub.2CCH CH(CH.sub.3).sub.2                            OC.sub.2 H.sub.5                                          O  N     56 CH.sub.2CCH CH(CH.sub.3).sub.2                            SCH.sub.3     O  N     57 CH.sub.2CCH CH.sub.2 Cl                            CH.sub.3      O  N     58 CH.sub.2CCH CH.sub.2 Cl                            OCH.sub.3     O  N     59 CH.sub.2CCH CH.sub.2 F                            CH.sub.3      O  N     60 CH.sub.2CCH CH.sub.2 F                            OCH.sub.3     O  N     61 CH.sub.2CCH CH.sub.2 F                            OC.sub.2 H.sub.5                                          O  N     62 CH.sub.2CCH CH.sub.2OCH.sub.3                            C.sub.2 H.sub.5                                          O  N     63 CH.sub.2CCH CH.sub.2SCH.sub.3                            OCH.sub.3     O  N     64 CH.sub.2CCH CH.sub.2SCH.sub.3                            CH.sub.3      O  N     65 CH.sub.2C CH                    CH.sub.2SCH.sub.3                            SCH.sub.3     O  N     66 CH.sub.2CCH CH.sub.2SCH.sub.3                            Cl            O  N     67 CH.sub.2CCH CH.sub.2SCH.sub.3                            OC.sub.2 H.sub.5                                          O  N     68 CH.sub.2CCH SCH.sub.3                            Cl            O  N  m.p. 139-140°     69 CH.sub.2CCH SCH.sub.3                            OCH.sub.3     O  N     70 CH.sub.2CCH SCH.sub.3                            C.sub.2 H.sub.5                                          O  N     71 CH.sub.2CCH SCH.sub.3                            OCH(CH.sub.3).sub.2                                          O  N     72 CH.sub.2CCH OCH(CH.sub.3).sub.2                            Cl            O  N     73 CH.sub.2CCH CF.sub.3                            OCH.sub.3     O  N     74 CH.sub.2CCH CF.sub.3                            CH.sub.3      O  N     75 CH.sub.2CCH CF.sub.3                            OC.sub.2 H.sub.5                                          O  N     76 CH.sub.2CCH CCl     OCH.sub.3     O  N     77 CH.sub.2CCH CCl.sub.3                            SCH.sub.3     O  N     78 CH.sub.2CCH CH.sub.3                            Cl            O  N     79 CH.sub.2CCH OCH.sub.3                            Cl            O  N  m.p. 148-154°     80 CH.sub.2CCH OCH.sub.3                            F             O  N     81 CH.sub.2CCH OCH.sub.3                            Br            O  N     82 CH.sub.2CCH CH.sub.3                            F             O  N     83 CH.sub.2C CH                    OCH.sub.3                            OCH.sub.3     O  CH     84 CH.sub.2CCH CH.sub.3                            CH.sub.3      O  N  m.p. 175-177°     85 CH.sub.2CCH OCH.sub.3                            OC.sub.2 H.sub.5                                          O  N     86 CH.sub.2CCH OCH.sub.3                            OC.sub.2 H.sub.5                                          O  CH     87 CH.sub.2CCH CH.sub.2OCH.sub.3                            OCH.sub.3     O  CH m.p. 162-163°     88 CH.sub.2CCH CH.sub.2OCH.sub.3                            OCH.sub.3     O  N     89 CH.sub.2CCH C.sub.2 H.sub.5                            OCH.sub.3     O  CH     90 CH.sub.2CCH CH.sub.2OCH.sub.3                            CH.sub.3      O  N     91 CH.sub.2CCH CH.sub. 3                            OCH.sub.3     S  N     92 CH.sub.2CCH OCH.sub.3                            OCH.sub.3     S  N     93 CH.sub.2CCH CH.sub.3                            OCH.sub.3     O  N  m.p. 157-158°     94 CH.sub.2CCH OCH.sub.3                            OCH.sub.3     O  N  m.p. 130-132°     95 CH.sub.2CCCH.sub.3                    CH.sub.2 Cl                            OCH.sub.3     O  N     96 CH.sub.2CCCH.sub.3                    CH.sub.2 F                            OCH.sub.3     O  N     97 CH.sub.2CCCH.sub.3                    CH.sub.3                            OCH.sub.3     O  CH     98 CH.sub.2CCCH.sub.3                    OCH.sub.3                            OCH.sub.3     O  CH     99 CH.sub.2CCCH.sub.3                    CH.sub.3                            CH.sub.3      O  CH     100        CH.sub.2C CCH.sub.3                    C.sub.2 H.sub.5                            OCH.sub.3     O  CH     101        CH.sub.2CCCH.sub.3                    OCH.sub.3                            Cl            O  CH     102        CH.sub.2CCCH.sub.3                    CH.sub.3                            Cl            O  CH     103        CH.sub.2CCCH.sub.3                    CF.sub.3                            OCH.sub.3     O  CH     104        CH.sub.2CCCH.sub.3                    CH.sub.2OCH.sub.3                            OCH.sub.3     O  CH     105        CH.sub.2CCCH.sub.3                    Br      OCH.sub.3     O  CH     106        CH.sub.2CCCH.sub.3                    Br      CH.sub.3      O  CH     107        CH.sub.2CCCH.sub.3                    OCH.sub.3                            SCH.sub.3     O  CH     108        CH.sub.2CCCH.sub.3                    CH.sub.3                            SCH.sub.3     O  CH     109        CH.sub.2CCCH.sub.3                    OCH.sub.3                            OC.sub.2 H.sub.5                                          O  CH     110        CH.sub.2CCCH.sub.3                    CH.sub.3                            CH.sub.3      O  N     111        CH.sub.2CCCH.sub.3                    CH.sub.3                            OCH.sub.3     O  N     112        CH.sub.2CCCH.sub.3                    OCH.sub.3                            OCH.sub.3     O  N     113        CH.sub.2CCCH.sub.3                    OCH.sub.3                            OC.sub.2 H.sub.5                                          O  N     114        CH.sub.2CCCH.sub.3                    C.sub.2 H.sub.5                            OCH.sub.3     O  N     115        CH.sub.2CCCH.sub.3                    C.sub.2 H.sub.5                            CH.sub.3      O  N     116        CH.sub.2CCCH.sub.3                    Cl      OCH.sub.3     O  N     117        CH.sub.2C CCH.sub.3                    OCH(CH.sub.3).sub.2                            OCH.sub.3     O  N     118        CH.sub.2CCCH.sub.3                    OCH(CH.sub.3).sub.2                            OCH.sub.3     O  N     119        CH.sub.2CCCH.sub.3                    OCH(CH.sub.3).sub.2                            CH.sub.3      O  N     120        CH.sub.2CCCH.sub.3                    OCH.sub.3                            SCH.sub.3     O  N     121        CH.sub.2CCCH.sub.3                    OC.sub.2 H.sub.5                            OC.sub.2 H.sub.5                                          O  N     122        CH.sub.2CCCH.sub.3                    OCH.sub.3                            CH.sub.2OCH.sub.3                                          O  N     123        CH.sub.2CH.sub.2CCH                    CH.sub.3                            OCH.sub.3     O  N     124        CH.sub.2CH.sub.2CCH                    CH.sub.3                            CH.sub.3      O  N     125        CH.sub.2CH.sub.2C CH                    C.sub.2 H.sub.5                            OCH.sub.3     O  N     126        CH.sub.2CH.sub.2CCH                    C.sub.2 H.sub.5                            CH.sub.3      O  N     127        CH.sub.2CH.sub.2CCH                    OCH.sub.3                            OCH.sub.3     O  N     128        CH.sub.2CH.sub.2CCH                    OCH.sub.3                            OC.sub.2 H.sub.5                                          O  N     129        CH.sub.2CH.sub.2CCH                    OC.sub.2 H.sub.5                            OC.sub.2 H.sub.5                                          O  N     130        CH.sub.2CH.sub.2CCH                    CH.sub.2OCH.sub.3                            OCH.sub.3     O  N     131        CH.sub.2CH.sub.2CCH                    CH.sub.3                            OCH.sub.3     O  CH     132        CH.sub.2CH.sub.2CCH                    OCH.sub.3                            OCH.sub.3     O  CH     133        CH.sub.2CH.sub.2C CH                    CH.sub.3                            CH.sub.3      O  CH     134        CH.sub.2CH.sub.2CCH                    CH.sub.2OCH.sub.3                            OCH.sub.3     O  CH     135        CH.sub.2CH.sub.2CCH                    CH.sub.3                            Cl            O  CH     136        CH.sub.2CH.sub.2CCH                    OCH.sub.3                            Cl            O  CH     137        CH.sub.2CH.sub.2CCH                    OCH.sub.3                            OC.sub.2 H.sub.5                                          O  CH     138        CH.sub.2 CCH                    CH.sub.3                            OCF.sub.2CHFCl                                          O  CH m.p. 153-155°     139        CH.sub.2CCH CH.sub.3                            OCF.sub.2CHF.sub.2                                          O  CH m.p. 171-173°     __________________________________________________________________________

                                      TABLE 3     __________________________________________________________________________      ##STR12##                                               Physical     No.        A            R.sub.1                            R.sub.3                                 R.sub.4  X E  data     __________________________________________________________________________     201        CH.sub.2CCH  6-Cl   CH.sub.3                                 OCH.sub.3                                          O N     202        CH.sub.2CCH  6-Cl   CH.sub.3                                 OCH.sub.3                                          O CH     203        CH.sub.2CCH  6-Cl   C.sub.2 H.sub.5                                 OCH.sub.3                                          O N     204        CH.sub.2CCH  6-Cl   OCH.sub.3                                 OCH.sub. 3                                          O CH     205        CH.sub.2CCH  6-Cl   OCH.sub.3                                 OCH.sub.3                                          O N     206        CH.sub.2CCCH.sub.3                     6-Cl   OCH.sub.3                                 CH.sub.3 O N     207        CH.sub.2CCCH.sub.3                     6-Cl   OCH.sub.3                                 CH.sub.3 O CN     208        CH.sub.2CH.sub.2CCH                     6-Cl   OCH.sub.3                                 CH.sub.3 O N     209        CH.sub.2CCH  6-OCH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O CH     210        CH.sub.2CCH  6-OCH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O N     211        CH.sub.2CCH  6-OCH.sub.3                            C.sub.2 H.sub.5                                 OCH.sub.3                                          O N     212        CH.sub.2CCH  6-OCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O N     213        CH.sub.2C CH 6-OCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O CH     214        CH.sub.2CCH  6-CH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O N     215        CH.sub.2CCH  6-CH.sub.3                            CH.sub.3                                 CH.sub.3 O CH     216        CH.sub.2CCH  6-CH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O CH     217        CH.sub.2CCH  6-CH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O N     218        CH.sub.2CCH  6-NO.sub.2                            CH.sub.3                                 OCH.sub.3                                          O N     219        CH.sub.2CCH  6-NO.sub.2                            CH.sub.3                                 OCH.sub.3                                          O CH     220        CH.sub.2CCH  6-NO.sub.2                            OCH.sub.3                                 OCH.sub.3                                          O CH     221        CH.sub.2CCH  6-NO.sub.2                            OCH.sub.3                                 OCH.sub.3                                          O N     222         CH.sub.2CCH 6-COOCH.sub.3                            OCH.sub.3                                 CH.sub.3 O CH     223        CH.sub.2CCH  6-COOCH.sub.3                            CH.sub.3                                 CH.sub.3 O N     224        CH.sub.2CCH  6-COOCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O N     225        CH.sub.2CCH  6-COOCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O CH     226        CH.sub.2CCH  5-Cl   CH.sub.3                                 OCH.sub.3                                          O N  m.p. 177°     227        CH.sub.2CCH  5-Cl   CH.sub.3                                 OCH.sub.3                                          O CH m.p. 208°     228        CH.sub.2CCH  5-Cl   OCH.sub.3                                 OCH.sub.3                                          O N     229        CH.sub.2CCH  5-Cl   OCH.sub.3                                 OCH.sub.3                                          O N     230        CH.sub.2CCH  5-Cl   C.sub.2 H.sub.5                                 CH.sub.3 O N     231        CH.sub.2CH.sub.2CCH                     5-Cl   CH.sub.3                                 OCH.sub.3                                          O N     232        CH.sub.2CH.sub.2CCH                     5-Cl   CH.sub.3                                 OCH.sub.3                                          O CH     233        CH.sub.2CCH.sub.3                     5-Cl   CH.sub.3                                 OCH.sub.3                                          O CH     234        CH.sub.2CCH.sub.3                     5-Cl   CH.sub.3                                 OCH.sub.3                                          O N     235        CH.sub.2CCH.sub.3                     5-Cl   C.sub.2 H.sub.5                                 OCH.sub.3                                          O N     236        CH.sub.2CCCH.sub.3                     5-Cl   OCH.sub.3                                 OCH.sub.3                                          O N     237        CH.sub.2CCCH.sub.3                     5-Cl   OCH.sub.3                                 OCH.sub.3                                          O CH     238        CH.sub.2CCH  5-F    CH.sub.3                                 OCH.sub.3                                          O N  m.p. 158°     239        CH.sub.2CCH  5-F    CH.sub.3                                 OCH.sub.3                                          O CH m.p. 211°                                               (decomp.)     240        CH.sub.2CCH  5-F    OCH.sub.3                                 C.sub.2 H.sub.5                                          O N     241        CH.sub.2CCH  5-F    OCH.sub.3                                 OCH.sub.3                                          O CH     242        CH.sub.2CCH  5-NO.sub.2                            OCH.sub.3                                 OCH.sub.3                                          O N     243        CH.sub.2CCH  5-NO.sub.2                            CH.sub.3                                 CH.sub.3 O N     244        CH.sub.2CCH  5-NO.sub.2                            CH.sub.3                                 OCH.sub.3                                          O CH     245        CH.sub.2CCH  5-CH(CH.sub.3).sub.2                            CH.sub.3                                 OCH.sub.3                                          O N     246        CH.sub.2CCH  5-CH(CH.sub.3).sub.2                            CH.sub.3                                 OCH.sub.3                                          O CH     247        CH.sub.2 CCH 5-CH(CH.sub.3).sub.2                            C.sub.2 H.sub.5                                 OCH.sub.3                                          O N     248        CH.sub.2CCH  5-CH(CH.sub.3).sub.2                            OCH.sub.3                                 OCH.sub.3                                          O N     249        CH.sub.2CH.sub.2CCH                     5-CH(CH.sub.3).sub.2                            OCH.sub.3                                 OCH.sub.3                                          O N     250        CH.sub.2CH.sub.2CCH                     5-CH(CH.sub.3).sub.2                            OCH.sub.3                                 CH.sub.3 O N     251        CH.sub.2CH.sub.2CCH                     5-CH(CH.sub.3).sub.2                            OCH.sub.3                                 OCH.sub.3                                          O CH     252        CH.sub.2CCCH.sub.3                     5-CH(CH.sub.3).sub.2                            OCH.sub.3                                 OCH.sub.3                                          O N     253        CH.sub.2CCCH.sub.3                     5-CH(CH.sub.3).sub.2                            OCH.sub.3                                 OCH.sub.3                                          O CH     254        CH.sub.2CCCH.sub.3                     5-CH(CH.sub.3).sub.2                            OCH.sub.3                                 CH.sub.3 O N     255        CH.sub.2CCCH.sub.3                     5-CH(CH.sub.3).sub.2                            OCH.sub.3                                 CH.sub.3 O CH     256        CH.sub.2CCH  5-CH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O N     257        CH.sub.2CCH  5-CH.sub.3                            CH.sub.3                                 OCHF.sub.2                                          O CH m.p. 201-203°     258        CH.sub.2CCH  5-CH.sub.3                            C.sub.2 H.sub.5                                 OCH.sub.3                                          O N     259        CH.sub.2CCH  5-CH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O N     260        CH.sub.2CCH  5-CH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O CH     261        CH.sub.2CCH  5-OCH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O CH     262        CH.sub.2CCH  5-OCH.sub.3                            OCH.sub. 3                                 OCH.sub.3                                          O CH     263        CH.sub.2CCH  5-OCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O N     264        CH.sub.2CCH  5-OCH.sub.3                            OCH.sub.3                                 C.sub.2 H.sub.5                                          O N     265        CH.sub.2CCH  5-COOCH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O N     266        CH.sub.2CCH  5-COOCH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O CH     267        CH.sub.2CCH  5-COOCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O N     268        CH.sub.2CCH  5-COOCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O CH     269        CH.sub.2CCH  3-NO.sub.2                            CH.sub.3                                 OCH.sub.3                                          O CH     270        CH.sub.2CCH  3-NO.sub.2                            CH.sub.3                                 OCH.sub.3                                          O N     271        CH.sub.2C CH 3-NO.sub.2                            C.sub.2 H.sub.5                                 OCH.sub.3                                          O N     272        CH.sub.2CCH  3-NO.sub.2                            OCH.sub.3                                 OCH.sub.3                                          O N     273        CH.sub.2CCH  3-OCH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O N     274        CH.sub.2CCH  3-OCH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O CH     275        CH.sub.2CCH  3-OCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O CH     276        CH.sub.2CCH  3-OCH.sub.3                            C.sub.2 H.sub.5                                 OCH.sub.3                                          O N     277        CH.sub.2CCH  3-OCH.sub.3                            OCH.sub.3                                 OCH.sub.3                                          O N     278        CH.sub.2CCH  3-CH.sub.3                            OCH.sub.3                                 CH.sub.3 O CH     279        CH.sub.2CCH  3-CH.sub.3                            C.sub.2 H.sub.5                                 CH.sub.3 O N     280        CH.sub.2CCH  3-CH.sub.3                            OCH.sub.3                                 CH.sub.3 O N     281        CH.sub.2CCH  3-CH.sub.3                            OCH.sub.3                                 CH.sub.3 O CH     282        CH.sub.2CCH  3-Cl   OCH.sub.3                                 CH.sub.3 O CH     283        CH.sub.2CCH  3-Cl   OCH.sub.3                                 CH.sub.3 O N     284        CH.sub.2CCH  3-Cl   OCH.sub.3                                 OCH.sub.3                                          O N     285        CH.sub.2CCH  3-Cl   OCH.sub.3                                 OCH.sub.3                                          O CH     286        CH.sub.2CCH  5-Br   OCH.sub.3                                 CH.sub.3 O N  m.p. 187-188°     287        CH.sub.2CCH  5-CH.sub.3                            CH.sub.3                                 OCH.sub.3                                          O N     288        CH.sub.2C CH 5-CH.sub.3                            OCH.sub.3                                 Cl       O CH m.p. 202-204°     289        CH.sub.2CCH  5-F    OCH.sub.3                                 OCH.sub.3                                          O N  m.p. 182-183°     290        CH.sub.2CCH  5-Cl   OCHF.sub.2                                 CH.sub.3 O CH m.p. 175-176°                                               (decomp.)     291        CH.sub.2CCH  5-F    OCHF.sub.2                                 CH.sub.3 O CH m.p. 175°                                               (decomp.)     292        CH.sub.2CCH  H      OCHF.sub.2                                 OCH.sub.3                                          O CH     293        CH.sub.2CCH  H      OCHF.sub.2                                 Cl       O CH     294        CH.sub.2CCH  H      CH.sub.3                                 OCF.sub.2CHF.sub.2                                          O CH     295        CH.sub.2CCH  H      OCH.sub.3                                 OCF.sub.2CHF.sub.2                                          O CH     296        CH.sub.2CCH  H      Cl   OCF.sub.2CHF.sub.2                                          O CH     297        CH.sub.2CCH  H      CH.sub.3                                 OCF.sub.2CHFCl                                          O CH     298        CH.sub.2CCH  H      OCH.sub.3                                 OCF.sub.2CHFCl                                          O CH     299        CH.sub.2CCH  H      Cl   OCF.sub.2CHFCl                                          O CH     300        CH.sub.2CCH  5-Cl   CH.sub.3                                 CH.sub.3 O CH m.p. 206-208°                                               (decomp.)     301        CH.sub.2CCH  5-F    CH.sub.3                                 CH.sub.3 O CH m.p. 219-220°                                               (decomp.)     __________________________________________________________________________

                                      TABLE 4     __________________________________________________________________________      ##STR13##                    Position     No.        A           of XA                         R.sub.1                               R.sub.2                                    X E  Physical data     __________________________________________________________________________     401        CH.sub.2CCH 5    2-CH.sub.3                               H    O N     402        CH.sub.2CCCH.sub.3                    5    2-CH.sub.3                               H    O CH     403        CH.sub.2CH.sub.2CCH                    5    2-CH.sub.3                               H    O CH     404        CH.sub.2 CH.sub.2CCH                    5    2-CH.sub.3                               H    O N     405        CH.sub.2CCCH.sub.3                    5    2-CH.sub.3                               H    O N     406        CH.sub.2CCH 5    2-CH.sub.3                               H    O CH     407        CH.sub.2CCH 5    2-Cl  H    O N  m.p. 175-176°     408        CH.sub.2CCH 5    2-Cl  H    O CH     409        CH.sub.2CCCH.sub.3                    5    2-Cl  H    O CH     410        CH.sub.2CCCH.sub.3                    5    2-Cl  H    O N     411        CH.sub.2CH.sub.2CCH                    5    2-Cl  H    O N     412        CH.sub.2CH.sub.2CCH                    5    2-Cl  H    O CH     413        CH.sub.2CH.sub. 2CCH                    5    2-CH.sub.3                               H    O N     414        CH.sub.2CCH 3    2-CH.sub.3                               H    O CH     415        CH.sub.2CCCH.sub.3                    3    2-CH.sub.3                               H    O CH     416        CH.sub.2CCH 3    2-CH.sub.3                               H    O N     417        CH.sub.2CCH 3    2-OCH.sub.3                               H    O CH     418        CH.sub.2CCH 3    2-OCH.sub.3                               H    O N     419        CH.sub.2CCCH.sub.3                    3    2-OCH.sub.3                               H    O N     420        CH.sub.2CCCH.sub.3                    3    2-OCH.sub.3                               H    O CH     421        CH.sub.2CH.sub.2CCH                    3    2-OCH.sub.3                               H    O CH     422        CH.sub.2CH.sub.2 CCH                    3    2-OCH.sub.3                               H    O N     423        CH.sub.2CCH 5    2-OCH.sub.3                               H    O N     424        CH.sub.2CCH 5    2-OCH.sub.3                               H    O CH     425        CH.sub.2CCCH.sub.3                    5    2-OCH.sub.3                               H    O CH     426        CH.sub.2CCCH.sub.3                    5    2-OCH.sub.3                               H    O N     427        CH.sub.2CH.sub.2CCH                    5    2-OCH.sub.3                               H    O N     428        CH.sub.2CH.sub.2CCH                    5    2-OCH.sub.3                               H    O CH     429        CH.sub.2CCH 3    5-Br  2-OCH.sub.3                                    O N     430        CH.sub.2CCH 3    5-Br  2-OCH.sub.3                                    O CH     431        CH.sub.2C CCH.sub.3                    3    5-Br  2-OCH.sub.3                                    O CH     432        CH.sub.2CCCH.sub.3                    3    5-Br  2-OCH.sub.3                                    O N     433        CH.sub.2CCH 3    5-COOCH.sub.3                               2-OCH.sub.3                                    O N     434        CH.sub.2CCH 3    5-COOCH.sub.3                               2-OCH.sub.3                                    O CH     435        CH.sub.2CH.sub.2CCH                    3    5-COOCH.sub.3                               2-OCH.sub.3                                    O CH     436        CH.sub.2CH.sub.2CCH                    3    5-COOCH.sub.3                               2-OCH.sub.3                                    O N     437        CH.sub.2CCH 3    5-COOCH.sub.3                               2-OCH.sub.3                                    O N     438        CH.sub.2CCH 3    5-COOCH.sub.3                               2-OCH.sub.3                                    O CH     439        CH.sub.2CCH 2    5-NO.sub.2                               3-CF.sub.3                                    O N     440        CH.sub. 2CCH                    2    5-NO.sub.2                               3-CF.sub.3                                    O CH     441        CH.sub.2CCH 2    5-NO.sub.2                               3-Cl O CH     442        CH.sub.2CCH 2    5-NO.sub.2                               3-Cl O N     443        CH.sub.2CCCH.sub.3                    2    5-NO.sub.2                               3-Cl O N     444        CH.sub.2CCCH.sub.3                    2    5-NO.sub.2                               3-Cl O CH     445        CH.sub.2CCH 2    5-CF.sub.3                               3-NO.sub.2                                    O CH     446        CH.sub.2CCH 2    5-CF.sub.3                               3-NO.sub.2                                    O N     447        CH.sub.2CCH 2    5-CH.sub.3                               3-CH.sub.3                                    O N     448        CH.sub.2CCH 2    5-CH.sub.3                               3-CH.sub.3                                    O CH     449        CH.sub.2CH.sub. 2CCH                    2    5-CH.sub.3                               3-CH.sub.3                                    O CH     450        CH.sub.2CH.sub.2CCH                    2    5-CH.sub.3                               3-CH.sub.3                                    O N     451        CH.sub.2CCH 2    5-Cl  3-NO.sub.2                                    O N     452        CH.sub.2CCH 2    5-Cl  3-NO.sub.2                                    O CH     453        CH.sub.2CCCH.sub.3                    2    5-Cl  3-NO.sub.2                                    O CH     454        CH.sub.2CCCH.sub.3                    2    5-Cl  3-NO.sub.2                                    O N     455        CH.sub.2CCH 2    5-Cl  3-Cl O N     456        CH.sub.2CCH 2    5-Cl  3-Cl O CH     457        CH.sub.2CCCH.sub.3                    2    5-Cl  3-Cl O CH     458        CH.sub.2C CCH.sub.3                    2    5-Cl  3-Cl O N     459        CH.sub.2CH.sub.2CCH                    2    5-Cl  3-Cl O N     460        CH.sub.2CH.sub.2CCH                    2    5-Cl  3-Cl O CH     461        CH.sub.2CH.sub.2CCH                    2    5-Br  3-OCH.sub.3                                    O N     462        CH.sub.2CH.sub.2CCH                    2    5-Br  3-OCH.sub.3                                    O CH     463        CH.sub.2CCH 3    5-Br  2-OCH.sub.3                                    O CH     464        CH.sub.2CCH 3    5-Br  2-OCH.sub.3                                    O N     465        CH.sub.2CCH 2    5-COOCH.sub.3                               3-OCH.sub.3                                    O N     466        CH.sub.2CCH 2    5-COOCH.sub.3                               3-OCH.sub.3                                    O CH     467        CH.sub.2C CCH.sub.3                    3    5-COOCH.sub.3                               2-OCH.sub.3                                    O CH     468        CH.sub.2CCCH.sub.3                    3    5-COOCH.sub.3                               2-OCH.sub.3                                    O N     469        CH.sub.2CH.sub.2CCH                    3    5-COOCH.sub.3                               2-OCH.sub.3                                    O N     470        CH.sub.2CH.sub.2CCH                    3    5-COOCH.sub.3                               2-OCH.sub.3                                    O CH     471        CH.sub.2CH.sub.2CCH                    3    5-CH.sub.3                               3-Br O CH     472        CH.sub.2CH.sub.2CCH                    2    5-CH.sub.3                               3-Br O N     473        CH.sub.2CCH 2    5-CH.sub.3                               3-Br O N     474        CH.sub.2CCH 2    5-CH.sub.3                               3-Br O CH     475        CH.sub.2CCH 2    5-Br  3-NO.sub.2                                    O N     476        CH.sub.2 CCH                    2    5-Br  3-NO.sub.2                                    O CH     477        CH.sub.2CCH 2    5-Cl  3-Br O N     478        CH.sub.2CCCH.sub.3                    2    5-Cl  3-Br O N     479        CH.sub.2CCCH.sub.3                    2    5-Cl  3-Br O CH     480        CH.sub.2CCH 2    5-Cl  3-Br O CH     481        CH.sub.2CH.sub.2CCH                    2    5-Cl  3-Br O N     482        CH.sub.2CCH 5    2-NO.sub.2                               H    O CH     483        CH.sub.2CCH 5    2-NO.sub.2                               H    O N     484        CH.sub.2CCH 5    2-Cl  H    O N     485        CH.sub.2CCH 5    2-Cl  H    O CH     486        CH.sub.2CCCH.sub.3                    5    2-Cl  H    O CH     487        CH.sub.2CCCH.sub.3                    5    2-Cl  H    O N     488        CH.sub.2CH.sub.2CCH                    5    2-Cl  H    O N     489        CH.sub.2CH.sub.2CCH                    5    2-Cl  H    O CH     __________________________________________________________________________

FORMULATION EXAMPLES EXAMPLE 3 Formulation Examples for active ingredients of the formula I (%=percent by weight)

    ______________________________________     (a) Wettable powder (a)     (b)      (c)     ______________________________________     active ingredient   20%     60%        0.5%     sodium lignin sulfonate                         5%      5%       5%     sodium lauryl sulfate                         3%      --       --     sodium diisobutylnaphthalene                         --      6%       6%     sulfonate     octylphenolpolyethylene glycol                         --      2%       2%     ether (7-8 mols of ethylene oxide)     highly dispersed silicic acid                         5%      27%      27%     kaolin              67%     --       --     sodium chloride     --      --        59.5%     ______________________________________

The active ingredient is well mixed with the additives and ground in a suitable mill. There are obtained wettable powders which can be diluted with water to give suspensions of the concentration desired.

    ______________________________________     (b) Emulsion concentrate                            (a)     (b)     ______________________________________     active ingredient      10%     1%     octylphenolpolyethylene glycol ether                            3%      3%     (4-5 mols of ethylene oxide)     calcium dodecyl benzene sulfonate                            3%      3%     castor oil polyglycol ether                            4%      4%     (36 mols of ethylene oxide)     cyclohexanone          30%     10%     xylene mixture         50%     79%     ______________________________________

Emulsions of the concentration desired can be obtained from this concentrate by dilution with water.

    ______________________________________     (c) Dust           (a)     (b)     ______________________________________     active ingredient   0.1%    1%     talcum             99.9%   --     kaolin             --      99%     ______________________________________

Dusts ready for use are obtained by mixing the active-ingredient with the carriers, and grinding the mixture in a suitable mill.

    ______________________________________     (d) Extruder granulate                         (a)     (b)     ______________________________________     active ingredient   10%     1%     sodium lignin sulfonate                         2%      2%     carboxymethylcellulose                         1%      1%     kaolin              87%     96%     ______________________________________

The active ingredient is mixed with the additives, and the mixture is then ground and moistened with water. It is extruded and subsequently dried in a stream of air.

    ______________________________________     (3) Coated granulate     ______________________________________     active ingredient    3%     polyethylene glycol (MG 200)                          3%     kaolin               94%     ______________________________________

The finely ground active ingredient is uniformuly applied, in a mixer, to the kaolin moistened with polyethylene glycol. Non-dusty coated granulates are obtained in this manner.

    ______________________________________     (f) Suspension concentrate                           (a)      (b)     ______________________________________     active ingredient     40%      5%     ethylene glycol       10%      10%     nonylphenolpolyethylene glycol                            6%      1%     ether (15 mols of ethylene oxide)     sodium lignin sulfonate                           10%      5%     carboxymethylcellulose                            1%      1%     37% aqueous formaldehyde solution                             0.2%     0.2%     silicone oil in the form of a                             0.8%     0.8%     75% aqueous emulsion     water                 32%      77%     ______________________________________

The finely ground active ingredient is intimately mixed with the additives. There is thus obtained a suspension concentrate from which can be produced, by dilution with water, suspensions of the concentration desired.

    ______________________________________     (g) Salt solution     ______________________________________     active ingredient      5%     isopropylamine         1%     octylphenolpolyethylene glycol ether                            3%     (78 mols of ethylene oxide)     water                  91%     ______________________________________

BIOLOGIGAL EXAMPLES EXAMPLE 4 Verification of the herbicidal activity before emergence of the plants

Plant seeds are sown in flower pots (12-15 cm diameter) in a greenhouse. The surface of the soil is treated immediately afterwards with an aqueous dispersion or solution of the active ingredients, the concentration used being 4 kg of active ingredient per hectare. The pots are then kept in the greenhouse at a temperature of 22°-25° C. with 50-70% relative humidity. The test results are evaluated after 3 weeks, and the action on the test plants is assessed according to the following scale of ratings:

1--plants have not emerged or are totally destroyed

2-3--very strong action

4-6--medium action

7-8--weak action

9 no action (as untreated control plants).

    ______________________________________     Pre-emergence action     Applied amount: 4 kg of active ingredient/hectare     Comp. No.  Avena   Setaria   Sinapis                                        Stellaria     ______________________________________      8         6       6         2     2     19         2       2         2     2     21         3       3         2     2     23         2       2         2     2     29         6       4         3     4     38         3       3         2     2     48         6       5         2     2     68         5       5         2     2     84         4       4         2     2     87         4       2         2     2     93         2       1         2     1     94         2       3         2     2     226        5       5         2     2     227        5       6         2     2     238*       4       5         2     2     239*       3       4         2     2     286        7       8         2     2     289*       6       6         2     2     407        6       6         3     3     ______________________________________      *Applied amount: 0.5 kg of active ingredient/hectare

EXAMPLE 5 Verification of selectivity on pre-emergence application

With the same test procedure as in Example 4, a number of varieties of plant seeds are treated with various applied amounts of active ingredient. The test results are evaluated according to the same scale of ratings.

    ______________________________________     Pre-emergence action:     Action     applied amount in     kg of AS*/hectare                   Comp. No. 23 Comp. No. 93     test plant    0.125  0.06      0.125                                         0.06     ______________________________________                   9      9         8    9     Alopecurus myos                   2      3         2    2     Echinochloa c.g.                   3      3         2    2     Rottboellia ex.                   8      9         4    4     Abutilon      2      2         2    2     Xanthium Sp.  2      3         6    6     Chenopodium Sp.                   3      3         2    2     Ipomoea       1      2         3    2     Sinapis       2      2         2    2     Galium aparine                   2      2         1    1     Viola tricolor                   3      4         2    2     ______________________________________      * = active substance

EXAMPLE 6 Demonstration of the herbicidal activity after emergence of the plants (contact action)

A number of weeds and cultivated plants, both monocotyledons and dicotyledons, are sprayed in the 4- to 6-leaf stage with an aqueous active-ingredient dispersion in dosages of 4 kg of active substance per hectare, and then kept at 24° to 26° C. with 45-60% relative humidity. The test results are evaluated 15 days after the treatment, and an assessment made according to the same scale of ratings as in the pre-emergence test.

    ______________________________________     Post-emergence action     Applied amount: 4 kg of active ingredient per hectare     Comp.                       Solan-      Stel-                                                  Phase-     No.   Avena   Setaria Lolium                                 um    Sinapis                                             laria                                                  olus     ______________________________________      8    8       8       3     3     2     3    3     19    2       4       3     2     2     3    3     21    5       4       4     2     2     2    4     23    2       3       2     2     2     2    2     38    4       5       2     2     2     2    3     48    6       5       4     2     2     2    4     68    6       6       2     3     2     2    3     84    6       5       2     2     2     2    3     87    5       5       2     3     2     3    4     93    4       2       4     2     2     3    3     94    4       3       2     2     2     2    4     226   7       7       3     3     3     3    4     227   7       8       4     3     3     4    4     238*  7       6       3     2     2     2    3     239*  4       4       2     3     2     3    3     289*  9       9       3     4     2     2    4     ______________________________________      *Applied amount: 0.5 kg of active ingredient per hectare

EXAMPLE 7 Verification of selectivity with post-emergence application

With the same test procedure as in Example 6, a largish number of plants are treated with various applied amounts of active ingredient. The test results are evaluated according to the scale of ratings given in Example 4.

    ______________________________________     Post-emergence action     Action     applied amount in     kg of AS/hectare                 Comp. No. 23                            Comp. No. 38                                       Comp. No. 93     test plants 0.125   0.06   0.125 0.06 0.125 0.06     ______________________________________     wheat       9       9      9     9    8     9     maize       3       3      4     5    9     9     rice (dry)  4       6      6     7    9     9     Alopecurus myos.                 3       3      4     4    1     2     Cyperus escul.                 9       9      3     3    4     9     soya-bean   2       2      6     6    9     9     cotton      4       4      7     7    9     9     Sinapis     2       3      2     2    1     1     Galium aparine                 4       4      4     4    1     1     Viola tricolor                 3       3      4     4    2     2     ______________________________________

EXAMPLE 8 Verification of sprouting inhibition on stored potatoes

A number of commercially available potatoes of the "Urgenta" variety, exhibiting no germination (sprouting), are washed and dried. The potatoes are afterwards each immersed for one minute in active-ingredient emulsions of varying concentration; they are then laid out on filter paper in plastic dishes, and stored at temperatures of 14° and 21° C. in darkness with 50% relative humidity, and an evaluation is made 34 days after application. At the same time the loss in weight of the tubers and the weight of the sprouts, compared with those values in the case of the untreated control specimens are determined. The compounds according to the invention brought about in this test a complete prevention of sprouting. The loss in weight of the potatoes was less than 10% of that of the control potatoes.

EXAMPLE 9 Verification of the reduction in growth of tropical leguminous cover crops

The test plants (centrosema plumieri and centrosema pubescens) are cultivated up to the fully grown stage, and then cut back to a height of 60 cm. After 7 days, the active substance is sprayed on in the form of an aqueous emulsion. The test plants are maintained at 70% relative humidity and with 6000 lux of artificial light, 14 hours per day, at temperatures of 27° by day and 21° C. by night. The test results are assessed 4 weeks after application of the emulsion. The new growth occurring compared with that on the control plants is estimated and weighed, and the phytotoxicity is evaluated. The plants treated with the active ingredients of the formula I show in this test a clear reduction in new growth (less than 20% of the new growth occurring on untreated control plants), without the test plants having suffered damage.

EXAMPLE 10 Regulation of growth of soya-beans

Soya-beans of the variety "Hark" are sown in plastic containers holding a soil/peat/sand mixture in the ratio of 6:3:1, and are placed into a climatic chamber. By optimum choice of temperature, illumination, fertiliser addition and watering, the plants develop over about 5 weeks into the 5-6 trifoliate stage. At this point, the plants are sprayed until thoroughly dripping wet with the aqueous liquor of an active ingredient of the formula I, the active-ingredient concentration being up to 100 g of AS/hectare. An assessment of the results is made about 5 weeks after application of the active ingredient. The active ingredients of the formula I produce a marked increase in the number and in the weight of the pods on the leading shoots compared with the number and weight of pods on the untreated control plants. 

What is claimed is:
 1. An N-phenylsulfonylcarbamate of the formula VII ##STR14## wherein A is a C₃ -C₆ alkynyl group,X is oxygen, sulfur or a sulfinyl or sulfonyl bridge, m is the number one or two, R₁ is hydrogen, halogen C₁ -C₅ -alkyl or C₂ -C₅ -alkenyl or a group --Y--R₅, R₂ is hydrogen, halogen, C₁ -C₅ -alkyl, C₂ -C₅ -alkenyl or C₁ -C₄ -haloalkyl, or a group --Y--R₅, --COOR₆, --NO₂ or --CO--NR₇ --R₈, R₅ and R₆ are each C₁ -C₅ -alkyl, C₂ -C₅ -alkenyl or C₂ -C₆ -alkynyl, R₇ and R₈ are each hydrogen, C₁ -C₅ -alkyl, C₂ -C₅ -alkenyl or C₂ -C₆ -alkynyl, and Y is oxygen, sulfur or a sulfinyl or sulfonyl bridge.
 2. A compound according to claim 1 wherein one --X--A group is in the 2-position with respect to the sulfonyl group.
 3. A compound according to claim 1 wherein one --X--A group is in each of the 2- and 5-positions with respect to the sulfonyl group.
 4. A compound according to claim 2 wherein R₁ is hydrogen, and R₂ is in the 5- or 6-position with respect to the sulfonyl group.
 5. A compound according to claim 4 wherein R₂ is hydrogen.
 6. A compound according to claim 5, wherein X is oxygen.
 7. A compound according to claim 6, wherein A is propargyl.
 8. A compound according to claim 1, wherein X is oxygen or sulfur, A is --CH₂ --C.tbd.CH, --CH₂ --C.tbd.C--CH₃ or --CH₂ --CH₂ --C.tbd.CH, the --X--A group occupies the 2-position, and m is the number one.
 9. N-(2-propargyloxyphenylsulfonyl)-phenylcarbamate according to claim
 7. 